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Efficacy Study of Cosmetic Product Against Telogen Effluvium on Women

Primary Purpose

Telogen Effluvium

Status

Completed

Phase

Not Applicable

Locations

France

Study Type

Interventional

Intervention

RV3466F lotion

Shampoo

About this trial

This is an interventional supportive care trial for Telogen Effluvium focused on measuring hair shedding, visual efficacy, visual effect, phototrichogram, pull test, 60-s hair count test, globalphotographs, Women

Eligibility Criteria

18 Years - 50 Years (Adult)FemaleDoes not accept healthy volunteers

Selection criteria :

Criteria related to the population:

Woman aged between 18 and 50 years old included
Phototype I to IV included, according to Fitzpatrick classification
Subject having signed written informed consent for the participation in the study
Subject affiliated to a social security system or health insurance, or is a beneficiary of either (if required by national regulation)
Subject whose last shampoo has been done at least 2 days before the selection visit
Use of a contraceptive method assessed as efficient by an investigator (including tubal ligation), started since at least 3 months before the selection visit, continued during the study and until after 1 month after the study end
Subject having hair length of at least 5 cm

Criteria related to diseases and hair loss disorder:

- Subject having effluvium telogen

Non selection criteria :

Criteria related to the population:

Pregnant or breastfeeding women or planning to being pregnant during the study
Perimenopausal symptoms (irregular menstruations, premenstrual syndrome …) or menopausal symptoms (climacteric troubles: hot flush, headaches, tiredness, insomnia, irritability …)
Menopause (absence of menstruations since at least 1 year) or a bilateral ovariectomy
Subject having frizzy hair
Subject who has forfeited her freedom by administrative or legal award or is under guardianship
Subject who, according to the judgement of the investigator, is unlikely to be compliant during the study
Subject unable to understand the information given (for linguistic or psychiatric reasons) and to give her consent in writing to participate
Subject who is currently participating in any another clinical trial
Subject who has participated in another clinical trial with hair product or treatment (local on the scalp and/or systemic) within the last 12 weeks before the selection visit

Criteria related to diseases and hair loss disorders:

- Subject who has any other hair disorder or hair disease (Ludwig II, III, AA, scarring alopecia …)

Criteria related to the population:

Pregnant or breastfeeding women or planning to being pregnant during the study
Perimenopausal symptoms (irregular menstruations, premenstrual syndrome …) or menopausal symptoms (climacteric troubles: hot flush, headaches, tiredness, insomnia, irritability …)
Menopause (absence of menstruations since at least 1 year) or a bilateral ovariectomy
Subject having frizzy hair
Subject who has forfeited her freedom by administrative or legal award or is under guardianship
Subject who, according to the judgement of the investigator, is unlikely to be compliant during the study
Subject unable to understand the information given (for linguistic or psychiatric reasons) and to give her consent in writing to participate
Subject who is currently participating in any another clinical trial
Subject who has participated in another clinical trial with hair product or treatment (local on the scalp and/or systemic) within the last 12 weeks before the selection visit

Criteria related to diseases and hair loss disorders:

Subject who has any other hair disorder or hair disease (Ludwig II, III, AA, scarring alopecia …)
History or clinical signs of hyperandrogenemia (menstrual cycle >35 days and hirsutism and signs of acne)
Inflammatory skin disease or progressive skin lesion on the scalp (psoriasis, seborrheic dermatitis, severe erythema, severe excoriation, severe sunburn, etc.).
Neoplastic disease at any time
History of hypersensitivity or intolerance to any of the following components applied by topical route: ethyl alcohol, components of the used hair dye, components of the RV3466F lotion
Thyroid disorders stabilised for less than 3 months

Criteria related to treatments and products:

Systemic treatment affecting the hair growth taken for more than 4 weeks during the last 12 weeks before the selection visit:
Finasteride
Dutasteride
Retinoids
Anti-mitotic, cytotoxic drugs other than antineoplastic
Spironolactone, flutamide, and all androgens
Anti-epileptic agents, interferon alpha
Minoxidil, Aminexil applied on the scalp within the last 24 weeks before the selection visit
Systemic or local anti hair loss treatment or product, taken or applied (cosmetic solution or capsules with vitamin B, zinc, caffeine…) within the last 4 weeks before the selection visit.
Drugs for thyroid disorders, if non stabilized for at least 3 months,
Iron supplement if not started for at least 3 months
Any hair care or styling method within the last week before the selection visit (e.g. dyeing, bleaching, perm, straightening, …)
Any hair care product applied on the scalp between the last shampoo and the selection visit (e.g. gel, hairspray, wax, foam, …) or water or brushing.
Any food supplements for hair growth taken for more than 4 weeks during the 12 weeks before the selection visit
Radiotherapy, chemotherapy at any time
Scalp surgery (hair transplants, laser) within the 12 months before the selection visit

Inclusion criteria :

Criteria related to hair loss disorder:
Subject having a proportion of hair in telogen phase superior to 15% (determined by phototrichogram at inclusion) on the centroparietal area of the scalp
Subject having a total hair density superior or equal to ≥ 220 hairs/ cm2 (determined by phototrichogram at inclusion) on the centroparietal area of the scalp

Non inclusion criteria :

Criteria related to treatments and products:
Any hair care product applied on the scalp between the selection visit and the inclusion visit (e.g. gel, hairspray, wax, foam, …) or water or brushing.
Reaction to the used hair dye during the inclusion visit

Sites / Locations

Centre de santé SABOURAUD C.E.P.C
INTERTEK

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Other

Arm Label

Treated group

Control group

Arm Description

This group will receive the RV3466F lotion and a neutral shampoo

This group will receive a neutral shampoo

Outcomes

Primary Outcome Measures

anagen to telogen ratio

From phototrichogram on the centroparietal area of the scalp

Secondary Outcome Measures

anagen to telogen ratio

From phototrichogram on the centroparietal area of the scalp

Density of telogen hair (number of hair in telogen phase/cm²)

From phototrichogram on the centroparietal area of the scalp

Density of anagen hair (number of hair in anagen phase/cm²)

From phototrichogram on the centroparietal area of the scalp

Total hair density (number of total hairs/cm²)

From phototrichogram on the centroparietal area of the scalp

Hair thickness

From phototrichogram on the centroparietal area of the scalp

Cumulative hair thickness

From phototrichogram on the centroparietal area of the scalp

Percentage of hairs pulled out

From the hair pull test on right and left bitemporal areas, frontal and occipital areas.

Total number of hairs shed

From the 60-s hair count test on the whole scalp

Efficacy and cosmetic acceptability questionnaire

Self-assessment questionnaire filled by the subjects. Ad-hoc questionnaires including numerical scale from 0-10 where higher scores mean a better outcome (improvement)

Density assessment

From globalphotographs of the centroparietal area with a stereotactic device, blinded and assessed by experts using a 7-points scale: Important aggravation (less dense)=-3; Moderate aggravation=-2; Mild aggravation=-1; Unchanged=0; Mild improvement=1; Moderate improvement=2; Important improvement (denser)=3

Full Information

NCT ID

NCT04652232

First Posted

November 20, 2020

Last Updated

November 26, 2020

Sponsor

Pierre Fabre Dermo Cosmetique

1. Study Identification

Unique Protocol Identification Number

NCT04652232

Brief Title

Efficacy Study of Cosmetic Product Against Telogen Effluvium on Women

Official Title

Randomized, Comparative Study to Assess the Effects of Cosmetic Lotion on Telogen Effluvium in Women Compared to a Control Group

Study Type

Interventional

2. Study Status

Record Verification Date

November 2020

Overall Recruitment Status

Completed

Study Start Date

December 5, 2016 (Actual)

Primary Completion Date

June 22, 2017 (Actual)

Study Completion Date

June 22, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title

Sponsor

Name of the Sponsor

Pierre Fabre Dermo Cosmetique

4. Oversight

Studies a U.S. FDA-regulated Drug Product

Studies a U.S. FDA-regulated Device Product

Data Monitoring Committee

5. Study Description

Brief Summary

Telogen effluvium (TE) is one of the most common causes of non-scarring diffuse hair loss, defined as global diminution of hair with no formation of areas completely bald. Premature termination of anagen into catagen and telogen hair follicle is the main mechanism observed in TE. It results in increased, synchronized telogen shedding leading to a decrease in global hair density. Acute telogen effluvium (ATE) has an abrupt onset and generalized scalp hair loss occurring 2-3 months after a triggering event, which could be unidentifiable in up to 33% cases. The degree of effluvium depends on the severity, duration of exposure and the type of agent, that can be: emotional stress, hormonal changes in the postpartum period, high fever, surgery, surgical/accidental trauma, severe haemorrhage, chronic systemic illness, or immense psychological stress, changes in medication or crash-diets. A summer effect possibly ultraviolet (UV) light induced, manifesting itself in autumn can cause ATE. The incidence of TE is not known, although it is likely that most women will experience at least 1 episode of TE during a lifetime. ATE can be diagnosed based on relevant medical and personal history and examination subjective complaints, clinical and physical exams or relevant investigations (hair pull test, phototrichogram, blood test…). ATE generates a lot of anxiety in the patient: significant impact on quality of life, self-esteem impairment, and stress increase. Thus, stress may act as a primary inducer; an aggravating factor or be a response to hair loss. ATE usually remits within few months (3-4 to 6 months) in 95% of cases if the trigger is removed or treated. Complete recovery may take until 1 year. A resolving TE is characterized by the absence of hair shedding, a negative hair pull test and synchronized hair growth. In this study, our aim is to assess the effects of the RV3466F lotion on hair growth, compared to a control group, with clinical and biometrological non- invasive methods on an adult female population with telogen effluvium.

Detailed Description

In order to evaluate the interest of the RV3466F lotion in the remission of ET, which occurs naturally when the triggering cause is stopped, ,a comparative controlled group is necessary. Moreover, due to the type of product (lotion) and the area of application ( scalp), the parallel groups design is adapted to the study purpose. To increase the adherence to the study protocol and to limit the negative psychological impact of hair shedding without treatment, the control group receive a neutral shampoo (extra mild shampoo). In order to avoid a bias between groups regarding the associated products, the same shampoo is given for the two groups. It should be used at the usual frequency. The allocation of the study product is randomized. Only women are included in the study as specified in the claim of the study product. The study area is the whole scalp. For evaluations the scalp is divided into 4 parts: centroparietal, parietal (right/left), frontal, and occipital areas The concerned part of the scalp which is evaluated can change according to the outcome measure. The Phototrichogram (PTG) is a painless, non-invasive and objective method, used done in 2 steps 48 hours apart to provide an accurate chronological following of hair growth on a specific scalp area . All data and images are computerized, which enables a semi-automatic quantification of hair growth variables (density, growth…). A preliminary dyeing of the hair is performed, in order to enhance the contrast between hair and scalp. The hair pull test is a semi quantitative method usually used to diagnose ongoing hair shedding and it helps to assess severity and location of hair loss. Global photographs help to illustrate the scalp hair coverage and the overall course of hair volume. For a better standardization of the shooting conditions, a stereotactic device is used, allowing their comparison from time to time, which is done ideally by trained people, the photographs being subsequently time blinded. The 60 seconds hair count test is a non-invasive and painless test performed by the subject itself, on the whole scalp in order to count the total number of hairs shed during a 60 seconds combing. The clinical study includes 9 visits: Visit 1 - Selection (D1) Visit 2 - Inclusion - 48 hours (±2h) after V1 Visit 3 - Intermediate - 4 weeks (D29 ± 4 days) Visit 4 -Intermediate - 48 hours (±2h) after V3 Visit 5 - Intermediate - 8 weeks (D57 ± 4 days) Visit 6 - Intermediate - 48 hours (±2h) after V5 Visit 7- Intermediate - 12 weeks (D85 ± 4 days) Visit 8 - Intermediate - 16 weeks (D113± 4 days) Visit 9 - Study end: 48 hours (±2h) after V8 The maximal duration of participation for a subject is 119 days.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study

Telogen Effluvium

Keywords

hair shedding, visual efficacy, visual effect, phototrichogram, pull test, 60-s hair count test, globalphotographs, Women

7. Study Design

Primary Purpose

Supportive Care

Study Phase

Not Applicable

Interventional Study Model

Parallel Assignment

Model Description

A randomisation list will be established. At the randomisation visit (Baseline visit 1), the Investigator will allocate a randomisation number to each subject according to the chronological order of inclusion. According to the list, the subject will be either randomized in one group of intervention. The investigator will only dispense the study product to the subjects included and randomized.

Masking

None (Open Label)

Allocation

Randomized

Enrollment

100 (Actual)

8. Arms, Groups, and Interventions

Arm Title

Treated group

Arm Type

Active Comparator

Arm Description

This group will receive the RV3466F lotion and a neutral shampoo

Arm Title

Control group

Arm Type

Other

Arm Description

This group will receive a neutral shampoo

Intervention Type

Other

Intervention Name(s)

RV3466F lotion

Intervention Description

Code: RV3466F Formula: MF5354 Application modalities: 3 times per week, in the evening, on a dry scalp 10 sprays overall hair after having achieved hair rays in order that the product is in contact with the scalp. Then massage to promote penetration of the lotion. Don't rinse. Shampoo should be avoided within the 2 hours after application

Intervention Type

Other

Intervention Name(s)

Shampoo

Intervention Description

Associated neutral shampoo: Extra mild shampoo Ducray® Code: RD0057H Formula: VS4031 Application modalities: as often as usual For the treated group only : no shampoo within the 2 hours after lotion application

Primary Outcome Measure Information:

Title

anagen to telogen ratio

Description

From phototrichogram on the centroparietal area of the scalp

Time Frame

Change from baseline to 16 weeks after application, for each group

Secondary Outcome Measure Information:

Title

anagen to telogen ratio

Description

From phototrichogram on the centroparietal area of the scalp

Time Frame

1 week, 4 weeks and 8 weeks after application, for each group

Title

Density of telogen hair (number of hair in telogen phase/cm²)

Description

From phototrichogram on the centroparietal area of the scalp

Time Frame

1 week, 4 weeks, 8 weeks and 16 weeks after application, for each group

Title

Density of anagen hair (number of hair in anagen phase/cm²)

Description

From phototrichogram on the centroparietal area of the scalp

Time Frame

1 week, 4 weeks, 8 weeks and 16 weeks after application, for each group

Title

Total hair density (number of total hairs/cm²)

Description

From phototrichogram on the centroparietal area of the scalp

Time Frame

1 week; 4 weeks, 8 weeks and 16 weeks after application, for each group

Title

Hair thickness

Description

From phototrichogram on the centroparietal area of the scalp

Time Frame

1 week, 4 weeks, 8 weeks and 16 weeks after application, for each group

Title

Cumulative hair thickness

Description

From phototrichogram on the centroparietal area of the scalp

Time Frame

1 week, 4 weeks, 8weeks and 16 weeks after application, for each group

Title

Percentage of hairs pulled out

Description

From the hair pull test on right and left bitemporal areas, frontal and occipital areas.

Time Frame

1 week, 4 weeks, 8 weeks 12 weeks and 16 weeks after application, for each group

Title

Total number of hairs shed

Description

From the 60-s hair count test on the whole scalp

Time Frame

4 weeks, 8 weeks 12 weeks and 16 weeks after application, for each group

Title

Efficacy and cosmetic acceptability questionnaire

Description

Self-assessment questionnaire filled by the subjects. Ad-hoc questionnaires including numerical scale from 0-10 where higher scores mean a better outcome (improvement)

Time Frame

1 week; 4 weeks, 8 weeks and 16 weeks after application, for each group

Title

Density assessment

Description

Time Frame

1 week and 16 weeks after application, for each group

10. Eligibility

Sex

Female

Minimum Age & Unit of Time

18 Years

Maximum Age & Unit of Time

50 Years

Accepts Healthy Volunteers

Eligibility Criteria

Selection criteria : Criteria related to the population: Woman aged between 18 and 50 years old included Phototype I to IV included, according to Fitzpatrick classification Subject having signed written informed consent for the participation in the study Subject affiliated to a social security system or health insurance, or is a beneficiary of either (if required by national regulation) Subject whose last shampoo has been done at least 2 days before the selection visit Use of a contraceptive method assessed as efficient by an investigator (including tubal ligation), started since at least 3 months before the selection visit, continued during the study and until after 1 month after the study end Subject having hair length of at least 5 cm Criteria related to diseases and hair loss disorder: - Subject having effluvium telogen Non selection criteria : Criteria related to the population: Pregnant or breastfeeding women or planning to being pregnant during the study Perimenopausal symptoms (irregular menstruations, premenstrual syndrome …) or menopausal symptoms (climacteric troubles: hot flush, headaches, tiredness, insomnia, irritability …) Menopause (absence of menstruations since at least 1 year) or a bilateral ovariectomy Subject having frizzy hair Subject who has forfeited her freedom by administrative or legal award or is under guardianship Subject who, according to the judgement of the investigator, is unlikely to be compliant during the study Subject unable to understand the information given (for linguistic or psychiatric reasons) and to give her consent in writing to participate Subject who is currently participating in any another clinical trial Subject who has participated in another clinical trial with hair product or treatment (local on the scalp and/or systemic) within the last 12 weeks before the selection visit Criteria related to diseases and hair loss disorders: - Subject who has any other hair disorder or hair disease (Ludwig II, III, AA, scarring alopecia …) Criteria related to the population: Pregnant or breastfeeding women or planning to being pregnant during the study Perimenopausal symptoms (irregular menstruations, premenstrual syndrome …) or menopausal symptoms (climacteric troubles: hot flush, headaches, tiredness, insomnia, irritability …) Menopause (absence of menstruations since at least 1 year) or a bilateral ovariectomy Subject having frizzy hair Subject who has forfeited her freedom by administrative or legal award or is under guardianship Subject who, according to the judgement of the investigator, is unlikely to be compliant during the study Subject unable to understand the information given (for linguistic or psychiatric reasons) and to give her consent in writing to participate Subject who is currently participating in any another clinical trial Subject who has participated in another clinical trial with hair product or treatment (local on the scalp and/or systemic) within the last 12 weeks before the selection visit Criteria related to diseases and hair loss disorders: Subject who has any other hair disorder or hair disease (Ludwig II, III, AA, scarring alopecia …) History or clinical signs of hyperandrogenemia (menstrual cycle >35 days and hirsutism and signs of acne) Inflammatory skin disease or progressive skin lesion on the scalp (psoriasis, seborrheic dermatitis, severe erythema, severe excoriation, severe sunburn, etc.). Neoplastic disease at any time History of hypersensitivity or intolerance to any of the following components applied by topical route: ethyl alcohol, components of the used hair dye, components of the RV3466F lotion Thyroid disorders stabilised for less than 3 months Criteria related to treatments and products: Systemic treatment affecting the hair growth taken for more than 4 weeks during the last 12 weeks before the selection visit: Finasteride Dutasteride Retinoids Anti-mitotic, cytotoxic drugs other than antineoplastic Spironolactone, flutamide, and all androgens Anti-epileptic agents, interferon alpha Minoxidil, Aminexil applied on the scalp within the last 24 weeks before the selection visit Systemic or local anti hair loss treatment or product, taken or applied (cosmetic solution or capsules with vitamin B, zinc, caffeine…) within the last 4 weeks before the selection visit. Drugs for thyroid disorders, if non stabilized for at least 3 months, Iron supplement if not started for at least 3 months Any hair care or styling method within the last week before the selection visit (e.g. dyeing, bleaching, perm, straightening, …) Any hair care product applied on the scalp between the last shampoo and the selection visit (e.g. gel, hairspray, wax, foam, …) or water or brushing. Any food supplements for hair growth taken for more than 4 weeks during the 12 weeks before the selection visit Radiotherapy, chemotherapy at any time Scalp surgery (hair transplants, laser) within the 12 months before the selection visit Inclusion criteria : Criteria related to hair loss disorder: Subject having a proportion of hair in telogen phase superior to 15% (determined by phototrichogram at inclusion) on the centroparietal area of the scalp Subject having a total hair density superior or equal to ≥ 220 hairs/ cm2 (determined by phototrichogram at inclusion) on the centroparietal area of the scalp Non inclusion criteria : Criteria related to treatments and products: Any hair care product applied on the scalp between the selection visit and the inclusion visit (e.g. gel, hairspray, wax, foam, …) or water or brushing. Reaction to the used hair dye during the inclusion visit

Overall Study Officials:

First Name & Middle Initial & Last Name & Degree

Yorik Dr DROUAULT

Organizational Affiliation

INTERTEK FRANCE

Official's Role

Principal Investigator

Facility Information:

Facility Name

Centre de santé SABOURAUD C.E.P.C

City

Paris

Country

France

Facility Name

INTERTEK

City

Paris

Country

France

12. IPD Sharing Statement

Plan to Share IPD

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Efficacy Study of Cosmetic Product Against Telogen Effluvium on Women

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